Canonical Allele Identifier: CA394370450

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2156610A>T (hg19) ; chr16:g.2106609A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106609A>T , CM000678.2:g.2106609A>T	GRCh38
NC_000016.9:g.2156610A>T , CM000678.1:g.2156610A>T	GRCh37
NC_000016.8:g.2096611A>T	NCBI36
NG_008617.1:g.34290T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7278T>A MANE Select	ENSP00000262304.4:p.Ser2426Arg
ENST00000262304.8:c.7278T>A	ENSP00000262304.4:p.Ser2426Arg
ENST00000415938.7:n.523T>A
ENST00000423118.5:c.7278T>A	ENSP00000399501.1:p.Ser2426Arg
ENST00000483024.1:c.446T>A
ENST00000483558.5:n.337T>A
ENST00000483731.5:n.1003T>A
ENST00000486339.6:n.1024T>A
ENST00000487932.5:c.1965T>A	ENSP00000457132.1:p.Ser655Arg
ENST00000496574.6:n.1281T>A
ENST00000565639.6:n.986T>A
ENST00000568591.5:c.2439T>A	ENSP00000457162.1:n.2439T>A
ENST00000569983.5:n.634T>A
NM_000296.3:c.7278T>A	NP_000287.3:p.Ser2426Arg
NM_001009944.2:c.7278T>A	NP_001009944.2:p.Ser2426Arg
XM_005255370.2:c.4233T>A	XP_005255427.1:p.Ser1411Arg
XM_011522525.1:c.7356T>A	XP_011520827.1:p.Ser2452Arg
XM_011522526.1:c.7356T>A	XP_011520828.1:p.Ser2452Arg
XM_011522527.1:c.7356T>A	XP_011520829.1:p.Ser2452Arg
XM_011522528.1:c.7332T>A	XP_011520830.1:p.Ser2444Arg
XM_011522529.1:c.7332T>A	XP_011520831.1:p.Ser2444Arg
XM_011522530.1:c.7302T>A	XP_011520832.1:p.Ser2434Arg
XM_011522531.1:c.7284T>A	XP_011520833.1:p.Ser2428Arg
XM_011522532.1:c.7230T>A	XP_011520834.1:p.Ser2410Arg
XM_011522533.1:c.7149T>A	XP_011520835.1:p.Ser2383Arg
XM_011522534.1:c.7092T>A	XP_011520836.1:p.Ser2364Arg
XM_011522535.1:c.5178T>A	XP_011520837.1:p.Ser1726Arg
XM_011522536.1:c.7356T>A	XP_011520838.1:p.Ser2452Arg
XM_011522537.1:c.4356T>A	XP_011520839.1:p.Ser1452Arg
XR_932867.1:n.7371T>A
XR_932868.1:n.7371T>A
XR_932869.1:n.7371T>A
XR_932870.1:n.7371T>A
XM_005255370.3:c.4233T>A	XP_005255427.1:p.Ser1411Arg
XM_011522528.3:c.7332T>A	XP_011520830.1:p.Ser2444Arg
XM_011522529.2:c.7332T>A	XP_011520831.1:p.Ser2444Arg
XM_011522537.2:c.4356T>A	XP_011520839.1:p.Ser1452Arg
XM_024450298.1:c.7398T>A	XP_024306066.1:p.Ser2466Arg
XM_024450299.1:c.7326T>A	XP_024306067.1:p.Ser2442Arg
XM_024450300.1:c.7188T>A	XP_024306068.1:p.Ser2396Arg
XM_024450301.1:c.5274T>A	XP_024306069.1:p.Ser1758Arg
NM_000296.4:c.7278T>A	NP_000287.4:p.Ser2426Arg
NM_001009944.3:c.7278T>A MANE Select	NP_001009944.3:p.Ser2426Arg